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The Medical Journal of Malaysia|September 6, 2000
Airway stenting for tracheal stenosisJ B Eng, L N Hooi, S H NgClinical Genetics|March 1, 1990
A case of 46,XX,r(X) (p1q1) diagnosed by in situ hybridizationJ Koch, S Kølvraa, N Hobolt, et al.American Journal of Medical Genetics|January 20, 1997
Limb defects in homozygous alpha-thalassemia: report of three casesD Chitayat, M M Silver, K O'Brien, et al.American Journal of Medical Genetics|September 20, 2001
Smith-Lemli-Opitz (RHS) syndrome: holoprosencephaly and homozygous IVS8-1G-->C genotypeM J Nowaczyk, S A Farrell, W L Sirkin, et al.The Canadian Nurse|April 1, 1996
Canuck place: a hospice for dying childrenB Davies, B Eng, R Arcand, et al.The Journal of Bone and Joint Surgery. American Volume|January 1, 1976
Mobility aids for the paraplegic childR M Letts, R Fulford, B Eng, et al.The Journal of Nutrition, Health & Aging|November 22, 2013
Hypoglycaemic symptoms and hypoglycaemia threshold in older people with diabetes--a patient perspectiveA H Abdelhafiz, C Bailey, B Eng Loo, et al.American Journal of Hematology|June 22, 2000
beta-thalassemia intermedia caused by compound heterozygosity for Hb Malay (beta codon 19 AAC-->AGC; asn-->Ser) and codons 41/42 (-CTTT) beta(0)-thalassemia mutationS K Ma, E Y Chow, A Y Chan, et al.Journal of Clinical Pathology|April 18, 2001
Should we screen for globin gene mutations in blood samples with mean corpuscular volume (MCV) greater than 80 fL in areas with a high prevalence of thalassaemia?L C Chan, S K Ma, A Y Chan, et al.Clinical and Laboratory Haematology|June 26, 2001
Haemoglobin Q-Thailand and hereditary spherocytosis in a Chinese familyK F Leung, W Y Au, A Y Chan, et al.Pageof 12